Reported Aug 6, 2025 · Ongoing

Sprinter Cart/Sprinter Cart XL Infusion Pole. Component used to hold 2 x 2 kg infusion bags.

Maquet Cardiopulmonary GmbH

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Maquet Cardiopulmonary Gmbh · Kehler Str. 31 · Rastatt · N/A

Is this the product you have?

  • Sprinter Cart/Sprinter Cart XL Infusion Pole. Component used to hold 2 x 2 kg infusion bags.
Lot codes and dates
  • Model No. 701033599
  • UDI4037691257860
Amount recalled
7,754 units

Where it was sold

  • Nationwide

Why it was recalled

Device does not comply with the labeling requirements of international standard IEC 60601-1.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 2:57 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.